The following data is part of a premarket notification filed by Jeil Medical Corporation with the FDA for Arix Hand System.
| Device ID | K161746 |
| 510k Number | K161746 |
| Device Name: | ARIX Hand System |
| Classification | Plate, Fixation, Bone |
| Applicant | Jeil Medical Corporation Seoul, KR 152-728 |
| Contact | Seungyong Lee |
| Correspondent | Seungyong Lee Jeil Medical Corporation Seoul, KR 152-728 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-06-24 |
| Decision Date | 2016-09-21 |
| Summary: | summary |